A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5509795



Internal ID286438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:40321713..40331713hg38UCSC Ensembl
chr14:40790917..40800917hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3810001
hg1910001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17696601
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5509795
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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